US11713277B2 - Glass or glass ceramic substrate provided with a decorative coating and method for producing same - Google Patents

Glass or glass ceramic substrate provided with a decorative coating and method for producing same Download PDF

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US11713277B2
US11713277B2 US16/388,126 US201916388126A US11713277B2 US 11713277 B2 US11713277 B2 US 11713277B2 US 201916388126 A US201916388126 A US 201916388126A US 11713277 B2 US11713277 B2 US 11713277B2
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layer
glass ceramic
substrate
ceramic substrate
coated glass
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US20190241467A1 (en
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Silke Knoche
Angelina Milanovska
Lutz Klippe
Ulf HOFFMANN
Ella Ruhl
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Schott AG
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Schott AG
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Priority claimed from DE102012103507.5A external-priority patent/DE102012103507B4/en
Priority claimed from DE201210109808 external-priority patent/DE102012109808A1/en
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Priority to US16/388,126 priority Critical patent/US11713277B2/en
Assigned to SCHOTT AG reassignment SCHOTT AG ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: HOFFMANN, ULF, KLIPPE, LUTZ, KNOCHE, SILKE, MILANOVSKA, ANGELINA, RUHL, ELLA
Publication of US20190241467A1 publication Critical patent/US20190241467A1/en
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    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C17/00Surface treatment of glass, not in the form of fibres or filaments, by coating
    • C03C17/34Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions
    • C03C17/42Surface treatment of glass, not in the form of fibres or filaments, by coating with at least two coatings having different compositions at least one coating of an organic material and at least one non-metal coating
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B05SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05DPROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D1/00Processes for applying liquids or other fluent materials
    • B05D1/36Successively applying liquids or other fluent materials, e.g. without intermediate treatment
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B05SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05DPROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D5/00Processes for applying liquids or other fluent materials to surfaces to obtain special surface effects, finishes or structures
    • B05D5/06Processes for applying liquids or other fluent materials to surfaces to obtain special surface effects, finishes or structures to obtain multicolour or other optical effects
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B05SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05DPROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D7/00Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials
    • B05D7/50Multilayers
    • B05D7/52Two layers
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C17/00Surface treatment of glass, not in the form of fibres or filaments, by coating
    • C03C17/006Surface treatment of glass, not in the form of fibres or filaments, by coating with materials of composite character
    • C03C17/008Surface treatment of glass, not in the form of fibres or filaments, by coating with materials of composite character comprising a mixture of materials covered by two or more of the groups C03C17/02, C03C17/06, C03C17/22 and C03C17/28
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C17/00Surface treatment of glass, not in the form of fibres or filaments, by coating
    • C03C17/28Surface treatment of glass, not in the form of fibres or filaments, by coating with organic material
    • C03C17/32Surface treatment of glass, not in the form of fibres or filaments, by coating with organic material with synthetic or natural resins
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C3/00Glass compositions
    • C03C3/04Glass compositions containing silica
    • C03C3/076Glass compositions containing silica with 40% to 90% silica, by weight
    • C03C3/089Glass compositions containing silica with 40% to 90% silica, by weight containing boron
    • C03C3/091Glass compositions containing silica with 40% to 90% silica, by weight containing boron containing aluminium
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C3/00Glass compositions
    • C03C3/04Glass compositions containing silica
    • C03C3/076Glass compositions containing silica with 40% to 90% silica, by weight
    • C03C3/089Glass compositions containing silica with 40% to 90% silica, by weight containing boron
    • C03C3/091Glass compositions containing silica with 40% to 90% silica, by weight containing boron containing aluminium
    • C03C3/093Glass compositions containing silica with 40% to 90% silica, by weight containing boron containing aluminium containing zinc or zirconium
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C2201/00Glass compositions
    • C03C2201/06Doped silica-based glasses
    • C03C2201/08Doped silica-based glasses containing boron or halide
    • C03C2201/10Doped silica-based glasses containing boron or halide containing boron
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C2201/00Glass compositions
    • C03C2201/06Doped silica-based glasses
    • C03C2201/30Doped silica-based glasses containing metals
    • C03C2201/34Doped silica-based glasses containing metals containing rare earth metals
    • C03C2201/36Doped silica-based glasses containing metals containing rare earth metals containing rare earth metals and aluminium, e.g. Er-Al co-doped
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C2201/00Glass compositions
    • C03C2201/06Doped silica-based glasses
    • C03C2201/30Doped silica-based glasses containing metals
    • C03C2201/40Doped silica-based glasses containing metals containing transition metals other than rare earth metals, e.g. Zr, Nb, Ta or Zn
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C2201/00Glass compositions
    • C03C2201/06Doped silica-based glasses
    • C03C2201/30Doped silica-based glasses containing metals
    • C03C2201/40Doped silica-based glasses containing metals containing transition metals other than rare earth metals, e.g. Zr, Nb, Ta or Zn
    • C03C2201/42Doped silica-based glasses containing metals containing transition metals other than rare earth metals, e.g. Zr, Nb, Ta or Zn containing titanium
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C2201/00Glass compositions
    • C03C2201/06Doped silica-based glasses
    • C03C2201/30Doped silica-based glasses containing metals
    • C03C2201/50Doped silica-based glasses containing metals containing alkali metals
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C2201/00Glass compositions
    • C03C2201/06Doped silica-based glasses
    • C03C2201/30Doped silica-based glasses containing metals
    • C03C2201/54Doped silica-based glasses containing metals containing beryllium, magnesium or alkaline earth metals
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C2217/00Coatings on glass
    • C03C2217/40Coatings comprising at least one inhomogeneous layer
    • C03C2217/425Coatings comprising at least one inhomogeneous layer consisting of a porous layer
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C2217/00Coatings on glass
    • C03C2217/40Coatings comprising at least one inhomogeneous layer
    • C03C2217/43Coatings comprising at least one inhomogeneous layer consisting of a dispersed phase in a continuous phase
    • C03C2217/46Coatings comprising at least one inhomogeneous layer consisting of a dispersed phase in a continuous phase characterized by the dispersed phase
    • C03C2217/48Coatings comprising at least one inhomogeneous layer consisting of a dispersed phase in a continuous phase characterized by the dispersed phase having a specific function
    • C03C2217/485Pigments
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C2217/00Coatings on glass
    • C03C2217/70Properties of coatings
    • C03C2217/72Decorative coatings
    • CCHEMISTRY; METALLURGY
    • C03GLASS; MINERAL OR SLAG WOOL
    • C03CCHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C2218/00Methods for coating glass
    • C03C2218/30Aspects of methods for coating glass not covered above
    • C03C2218/36Underside coating of a glass sheet
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F24HEATING; RANGES; VENTILATING
    • F24CDOMESTIC STOVES OR RANGES ; DETAILS OF DOMESTIC STOVES OR RANGES, OF GENERAL APPLICATION
    • F24C15/00Details
    • F24C15/02Doors specially adapted for stoves or ranges
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F24HEATING; RANGES; VENTILATING
    • F24CDOMESTIC STOVES OR RANGES ; DETAILS OF DOMESTIC STOVES OR RANGES, OF GENERAL APPLICATION
    • F24C15/00Details
    • F24C15/10Tops, e.g. hot plates; Rings
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/24Structurally defined web or sheet [e.g., overall dimension, etc.]
    • Y10T428/24355Continuous and nonuniform or irregular surface on layer or component [e.g., roofing, etc.]
    • Y10T428/24364Continuous and nonuniform or irregular surface on layer or component [e.g., roofing, etc.] with transparent or protective coating

Definitions

  • the invention relates to a method for producing a decorative coating on a glass or glass ceramic substrate and to a glass or glass ceramic substrate produced according to such method. More particularly, the invention relates to a glass ceramic cooktop having a bottom surface coating.
  • Glass and glass ceramic substrates with a decorative coating are known from practice.
  • a problem with such coatings is that the layer system is subjected to high thermal loads.
  • the coatings When used for induction cooktops, for example, the coatings have to resist temperatures of up to 500° C.
  • a drawback is that sputtering of metallic layers is quite complex. In particular if it is desired to only partially cover the substrate with a decorative layer, for example in order to mark cooking zones, additional process steps for masking are necessary.
  • Another drawback is due to the fact that there are only few possibilities to vary the visual appearance of the coating, in particular in terms of the desired color. For example it is very complex to apply black layers using a sputtering process.
  • enamel coatings have the advantage that by selecting the employed pigments which are added to the glass flux material almost any color can be produced.
  • known glass flux-based coatings can usually only be applied in a limited layer thickness with the resulting opacity and are prone to cracking, which has a significant impact on the visual appearance of the layer.
  • known enamel layers put the employed substrate under tension thus reducing its strength.
  • porous enamel layers In order to prevent cracking and to improve the mechanical strength of the composite material produced, it is known to apply porous enamel layers.
  • a drawback of these layers is that the pores are in the range of the wavelength of visible light, so that a matt appearance is caused.
  • EP 1 435 759 B1 describes a method for applying a decorative coating onto a cooktop, in which a dense layer containing inorganic pigments is applied to the upper surface and a porous layer containing inorganic pigments to the bottom surface. The intention therein is to avoid cracks in the bottom layer by all means.
  • sol-gel also known are coatings produced by a sol-gel process in which at least one pigment or filler is added to the sol-gel material.
  • sol-gel layers are also prone to delamination or cracking, which is then manifested as a local lightening on the composite material.
  • luster paints as a decorative coating.
  • a drawback with luster paints is that the selection of the color location is limited and that at least for dark, especially for black coatings noble metal based paints have to be used, which involves increased manufacturing costs.
  • the invention is based on the object to provide a method for applying a decorative coating to glass or ceramic substrates, which permits to easily provide the substrate with a heat-resistant layer.
  • a more particular object of the invention is to provide for free selection of the color location of the coating and for application of a glossy layer.
  • the object of the invention is already achieved by a method for applying a decorative coating to a glass or glass ceramic substrate and by a coated glass or glass ceramic substrate.
  • the invention relates to a method for applying a decorative coating to a glass or glass ceramic substrate.
  • a decorative coating refers to any coating that changes the visual appearance of the substrate.
  • the coating is opaque or semi-transparent.
  • the coating may be of any desired color.
  • a transparent and/or heat-resistant material is used as the glass or glass ceramic substrate.
  • glass ceramics which are known as so-called zero-expansion material, it is also conceivable for the invention to be employed for heat-resistant glasses.
  • a glass ceramic substrate will usually be used.
  • a transparent substrate refers to a substrate which is at least partially transparent in the visible range.
  • the substrate is preferably planar. However, it is also conceivable to use the invention for curved substrates, e.g. those used for fireplace windows.
  • a first layer having a textured surface is initially applied using a glass flux.
  • a textured surface refers to a surface that has a surface relief. That means, the applied coating is not flat but has valleys and mountains.
  • the texture depth is preferably in the micrometer range. In particular, a maximum texture depth from 0.1 to 5 ⁇ m, preferably from 0.2 to 3 ⁇ m, and more preferably from 0.5 to 2 ⁇ m is contemplated.
  • the texture depth may be determined, for example, by measuring the surface profile of a sample material along 10 randomly selected test sections of a length of 1 cm, for example by scanning electron microscopy.
  • the average value of the 10 maximum height differences so determined represents the maximum texture depth for the purposes of the invention.
  • Such a textured surface is achieved by adding pigment and/or filler particles to the material employed for the coating, as will be explained in more detail below.
  • a further layer is applied onto the textured first layer, which at least partially and more preferably completely fills the textured surface, so that the material of the first layer gradually merges into the material of the second layer. It is also conceivable to fill the first layer with the layer material of the second layer only in sections of the first layer.
  • the material composition of the layer system comprised of the two materials changes, starting from the substrate up to the surface of the coating, in that a higher proportion of the material of the first layer is present at the surface of the substrate (preferably approximately 100%), whereas on the surface of the layer system the proportion of the material of the first layer is smaller (preferably approximately 0%).
  • the inventors have found that under thermal load the resulting layer system is much less prone to clearly visible changes, in particular to light stains caused by cracking.
  • intended cracking may even cause a generation of zones of increased temperature resistance, which results in enhance temperature resistance of the entire layer system. This is especially true in case of a first layer produced by glass flux onto which a polymer layer is applied.
  • the layer system consisting of the first and the further layer may be applied onto a layer having a high texture depth of several microns.
  • This may in particular be a layer deposited by a sol-gel process.
  • a further textured layer of high textural depth of preferably more than 10 ⁇ m it is possible to produce patterns, haptic grip surfaces etc., for example. These may in particular be arranged on the bottom surface of a substrate, in particular of a cooktop.
  • the material of the first and/or second layer comprises pigments, in particular in a proportion of more than 50% (% values always given in percent by weight, unless otherwise indicated).
  • the layer used as the first layer preferably has a high pigment content of more than 60%.
  • metal oxides are used as the pigments. These may in particular include: cobalt oxides/spinels, cobalt-aluminum spinels, cobalt-titanium spinels, cobalt-chromium spinels, cobalt-nickel-manganese-iron-chromium oxides/spinels, cobalt-nickel-zinc-titanium-aluminum oxides/spinels, iron oxides, iron-chromium oxides, iron-chromium-zinc-titanium oxide, copper-chromium spinels, nickel-chromium-antimony-titanium oxides, titanium oxides, zirconium-silicon-iron oxides/spinels etc.
  • any conceivable absorption pigments are also eligible as the pigments, in particular platelet- or rod-shaped pigments. It is also possible to use coated effect pigments.
  • fillers in particular to the first layer which fillers may especially include: SiO 2 particles, alumina particles, fumed silica, soda-lime, alkali-aluminosilicate or borosilicate glass spheres, hollow glass spheres.
  • a layer with a high texture depth will be formed.
  • the layer is baked at such a high temperature that the glass flux particles melt while the filler and/or pigment particles substantially remain intact, so as to obtain a dense layer having a high texture depth.
  • a dense layer in particular refers to a layer having a closed porosity of less than 5%.
  • a semi-transparent rough first layer is formed, which is filled with a polymer layer as the further layer in order to provide, in combination, an opaque glossy bottom surface coating.
  • This semi-transparent area may in particular serve for integrating a display.
  • the use of a screen printing process for applying the further layer permits to easily produce the recessed areas.
  • the recessed area may yet contain further, third layer materials.
  • the layer thickness of the first layer is preferably between 0.1 and 10 ⁇ m, more preferably between 1 and 5 ⁇ m.
  • the further layer preferably has a thickness from 1 ⁇ m to 100 ⁇ m.
  • the maximum texture depth of the first layer is preferably more than 40%, more preferably more than 80%, and most preferably more than 90% of the maximum layer thickness.
  • crystalline or glassy inorganic materials may be used as a glass flux material of the first layer.
  • the glass flux material is preferably provided in particulate form and is optionally mixed with the pigment and/or filler particles.
  • the glasses preferably used are silicate glasses such as borosilicate glasses, zinc-borosilicate glasses, bismuth-borosilicate glasses, silicon oxide glasses, zinc-silicate glasses, bismuth-silicate glasses, aluminosilicate glasses, invert glasses, or borate and phosphate glasses, such as zinc-borate glasses, bismuth-borate glasses.
  • silicate glasses such as borosilicate glasses, zinc-borosilicate glasses, bismuth-borosilicate glasses, silicon oxide glasses, zinc-silicate glasses, bismuth-silicate glasses, aluminosilicate glasses, invert glasses, or borate and phosphate glasses, such as zinc-borate glasses, bismuth-borate glasses.
  • the first layer is preferably baked at a temperature of more than 500° C., most preferably of more than 600° C.
  • “Baking” in the meaning of the invention refers to curing of the coating material.
  • the material is in particular baked at such a high temperature that the glass flux material melts and does not only sinter.
  • the heating is preferably performed so rapidly and temporarily that the glass flux material densifies without bringing about any evaporation processes to occur, which might cause pore formation.
  • the glass flux material has to be that fluid that it completely wets the settled pigment particles and/or fillers.
  • the layer material used for the further layer is preferably a polymer.
  • a polysiloxane, polysilsesquioxane, polyurethane, epoxy- and/or polyester-functionalized silicone resins, or a sol-gel may be used.
  • the further layer is also mixed with pigments, in particular inorganic pigments and/or fillers and/or organic colorants.
  • the fillers used include in particular silica particles, alumina particles, fumed silica, soda-lime, alkali-alumosilicate or borosilicate glass spheres, hollow glass spheres.
  • Pigments that come into consideration include any conceivable absorption pigments, in particular platelet- or rod-shaped pigments.
  • Colorants that may be used include any organic colorants which are sufficiently temperature stable.
  • transparent layer material may be used for the second layer, which may however even be colorized in order to reduce the color contrast between the opaque part and the display area.
  • various coloring agents may be used which provide a semi-transparent coating with low scattering.
  • organic colorants may be added to the coating material.
  • Orasol® RLi may be used.
  • Temperature resistant colorants that are also suitable include azo dyes such as methyl orange, alizarin yellow or Congo red; triphenylmethane dyes such as malachite green, eosin, fluorescein, aurin, and phenolphthalein; Vat dyes such as anthraquinone dyes, indigo, and thioindigo; fluorescent dyes; perylene dyes.
  • phthalocyanines with e.g. Cr, Cu, Ni, Zn, or Co as the central atom may be employed.
  • a dense, optionally glossy, thermally highly resistant layer system is obtained.
  • This resulting gradient layer has a porosity of less than 7 vol % and is thus dense. This value can be determined in a cross section. Nitrogen sorption according to BET reveals surface areas of the layer system of less than 5 m 2 /g, which again is evidence of a dense gradient composite.
  • the invention in particular permits in a very simple way to produce black glossy layers of high thermal resistance.
  • the layers are in particular resistant to a short-term temperature load of more than 500° C. and to a long-term exposure to more than 400° C.
  • black layers can be produced by combining a first and a further layer, which when individually applied each have a lightness L in the Lab color space of more than 29.0. That means, these layers are rather gray and do not exhibit the desired black color appearance.
  • a combination of these layers results in a lightness L of less than 28.0, in particular less than 27.0.
  • the application of the layer material of the first and/or further layer is preferably accomplished using a printing technique, in particular by screen printing.
  • the use of a screen printing process permits to only partially coat the substrate. That means, it is possible to print only certain areas while other areas are left out. In case of a cooktop, in particular the display areas or the hobs may be left out.
  • the invention further relates to a coated glass or glass ceramic substrate which can be produced as described above.
  • FIG. 1 is a schematic cross-sectional view of the glass or glass ceramic of the present disclosure.
  • FIG. 2 shows a schematic flow chart of the essential method steps.
  • FIG. 3 shows photographs of different samples of coated glass ceramic substrates according to the present disclosure.
  • FIG. 4 shows the spectral transmittance curve of a glass ceramic substrate coated with component A according to the embodiment of Example 1 of the invention.
  • FIG. 5 illustrates the lightness value (L value) in the Lab system of the samples shown in FIG. 3 .
  • FIG. 6 illustrates the change in color location due to rear printing with different colors.
  • FIG. 7 shows a scanning electron micrograph, from a top view, of a glass flux based coating material for the first layer which was baked at 680° C. at 1,000 times magnification.
  • FIG. 8 shows a scanning electron micrograph, from the top view, of the glass flux based coating material of FIG. 7 at 5,000 times magnification.
  • FIG. 9 shows a scanning electron micrograph, from the top view, of the glass flux based coating material of FIG. 7 at 100,000 times magnification.
  • FIG. 10 shows a scanning electron micrograph, from a sectional view, of the glass flux based coating material of FIG. 7 at 50,000 times magnification.
  • FIG. 11 shows a scanning electron micrograph, from a top view, of a first layer with a pigment content of 70%, which was baked at 725° C. at 20,000 times magnification.
  • FIG. 12 shows a scanning electron micrograph, from a sectional view, of the first layer of FIG. 11 at 50,000 times magnification.
  • FIG. 13 shows a scanning electron microscope cross-sectional view of a first layer with a pigment content of 65% baked at 680° C. at 10,000 times magnification.
  • FIG. 14 shows a scanning electron microscope cross-sectional view of a first layer with a pigment content of 70% baked at 725° C. at 10,000 times magnification.
  • FIGS. 1 to 14 The invention will now be described with reference to the drawings of FIGS. 1 to 14 .
  • FIG. 1 is a schematic cross-sectional view which serves to illustrate the effect of the invention.
  • a coated glass or glass ceramic substrate 1 can be seen which consists of the substrate 2 and a gradient layer.
  • the gradient layer comprises a first layer 3 applied using a glass flux, which layer contains more than 60% of pigment particles and small filler particles.
  • a textured surface is formed which is filled with a polysiloxane layer as a further layer 4 .
  • the further layer 4 also contains pigment particles.
  • the gradient layer is used as a bottom surface coating, that means the viewer will look at the gradient layer from the side opposite layers 3 and 4 .
  • the gradient layer is preferably black and glossy.
  • layers may be applied as described in the examples below.
  • the layer material used for the first layer has a composition according to component A, and the further layer has a composition according to component B.
  • crystalline and/or glassy inorganic materials can be used.
  • these basic glasses may be of siliceous origin, such as e.g. borosilicate glasses, fused silica glasses, zinc-silicate glasses, zinc-borosilicate glasses, bismuth-silicate glasses, bismuth-borosilicate glasses, alumosilicate glasses, soda-lime glasses, or borate, zinc-borate, bismuth-borate glasses, or phosphate glasses, and invert glasses.
  • siliceous origin such as e.g. borosilicate glasses, fused silica glasses, zinc-silicate glasses, zinc-borosilicate glasses, bismuth-silicate glasses, bismuth-borosilicate glasses, alumosilicate glasses, soda-lime glasses, or borate, zinc-borate, bismuth-borate glasses, or phosphate glasses, and invert glasses.
  • glasses of the following composition may include, for example, glasses of the following composition:
  • Component A is applied to the bottom surface of a transparent glass ceramic plate of the type CERAN CLEARTRANS® (size 250 ⁇ 300 mm, thickness 4 mm) over the entire surface by screen printing (180 mesh screen), and is baked at 725° C. for 10 min in a continuous furnace.
  • Component A comprises 35% of zinc-borosilicate glass (softening point T s of 575° C.) and 65% of a black pigment (Cu—Cr spinel; CuCr 2 O 4 ), both components having a grain size of D50 ⁇ 5 ⁇ m.
  • a sample was measured in a spectrometer “Lambda 900” from company Perkin Ellmer, with and without Ulbricht sphere. At a wavelength of 550 nm, the transmittance was 11% with Ulbricht sphere and 1% without sphere, which means the sample exhibits a high level of scattered light.
  • component B1 which forms the further layer is applied on component A by screen printing, also to the entire surface area.
  • a black silicone paint is used as the component B1, for example that described in published patent application DE 10 2010 031 866 A1. This paint is printed using a 77 mesh screen, and is then dried at 200° C. for 45 min.
  • the spectrometer “Lambda 950” from company Perkin Ellmer was used to measure both the individual layer of component A and the gradient layer including components A and B1 in reflection. The difference in haze values is 5.5%, that means the reflection measurements confirmed that the layer consisting of component A has a high scattering power, while the gradient composite exhibits almost no scattering behavior.
  • the gradient layer so produced consisting of the materials of components A and B, meets the requirements for a cooktop with a short-term temperature load of up to 500° C.
  • component B1 may have a composition as follows:
  • Component A is applied to the bottom surface of a transparent glass ceramic plate of the type CERAN CLEARTRANS® (size 250 ⁇ 300 mm, thickness 4 mm) over the entire surface by screen printing and is baked in a continuous furnace at 750° C. for 15 min.
  • Component A comprises 25% of borosilicate glass (T s of about 620° C.) and 75% of black pigment (Cu—Cr spinel), with grain sizes of D50 ⁇ 5 ⁇ m.
  • component B2 is applied on component A by screen printing (77 mesh screen), likewise to the entire surface area, and is dried at 230° C. for 90 min.
  • a gray silicone paint is used as the component B2.
  • the so produced plate with the gradient layer satisfies the requirements for a cooktop with a short-term temperature load of up to 500° C.
  • component B2 may have a composition as follows:
  • Component A is applied to the bottom surface of a transparent glass ceramic plate of the type CERAN CLEARTRANS® (size 250 ⁇ 300 mm, thickness 4 mm) over the entire surface by screen printing (180 mesh screen) and is then dried.
  • Component A comprises 90% of borosilicate glass (T s of about 755° C.) and 10% of an effect pigment (Merck, type Xirallic®—crystal silver), mixed with screen printing medium.
  • component B is applied onto component A by screen printing (140 mesh screen), also to the entire surface area, and is dried at 825° C. for 10 min.
  • Component B comprises 30% of zinc-borosilicate glass (T s of about 575° C.) and 70% of a black pigment (Fe—Ni—Cr spinel), grain sizes D50 ⁇ 5 ⁇ m.
  • This paint is printed using a 77 mesh screen, and is then dried at 230° C. for 45 min.
  • the resulting gradient layer including components A, B, and C is smooth, dense, and, when viewed from the upper side, black with glitter effect.
  • Component A may also be produced using borosilicate glasses of different composition with varying contents of effect pigments (e.g. 1-10%). In this way, the visual appearance may be changed, e.g. as black with gold glitter or black with stainless steel color glitter.
  • the gradient layers so produced satisfy the requirements for a cooktop with a short-term temperature load of up to 500° C.
  • a sol-gel paint (preparation described in published patent application WO2010/081531 A1) including 25% of effect pigment (Merck, type Iriodin®; particle size ⁇ 25 ⁇ m) is applied to the bottom surface of a transparent glass ceramic plate of the type CERAN CLEARTRANS® (size 250 ⁇ 300 mm, thickness 4 mm) over the entire surface thereof by screen printing, 140 mesh screen, in form of geometric patterns and labeling, and is dried at 150° C. for 10 min to obtain a layer thickness of 8 ⁇ m. Subsequently, the gradient layer is produced in the manner as described in Example 1.
  • the plates thus produced meet the requirements for a cooktop with a short-term temperature load of up to 500° C.
  • Component A is applied to the bottom surface of a plurality of transparent glass ceramic plates of the type CERAN CLEARTRANS® (size 250 ⁇ 300 mm, thickness 4 mm) over the entire surface by screen printing (100 mesh screen), and is baked at 725° C. for 10 min.
  • Component A comprises 35% of zinc-borosilicate glass (T s of about 575° C.) and 65% of a white pigment (TiO 2 ), with grain sizes of D50 ⁇ 5 ⁇ m.
  • components B1, B2, and B3 are applied to different plates over component A by screen printing, likewise to the entire surface area thereof and using a 77 mesh screen, and then are dried at 200° C. for 45 min.
  • the plates with the gradient layers so produced satisfy the requirements for a cooktop with a short-term temperature load of up to 500° C.
  • component B3 may have a composition as follows:
  • Component A is applied to the bottom surface of a transparent glass ceramic plate of the type CERAN CLEARTRANS® (size 250 ⁇ 300 mm, thickness 4 mm) over the entire surface thereof by screen printing, and is baked at 800° C. for 30 min.
  • Component A comprises 70% of borosilicate glass (T s of about 820° C.) and 30% of a black pigment (Cr—Fe—Ni—Mn spinel), grain sizes of D50 ⁇ 5 ⁇ m.
  • component B1 is applied on component A by screen printing (77 mesh screen), likewise to the entire surface area thereof, and is dried at 200° C. for 90 min.
  • Component A is applied to the bottom surface of a transparent, non-ceramized glass plate of the type CERAN CLEARTRANS® (size 250 ⁇ 300 mm, thickness 4 mm) over the entire surface thereof by screen printing (180 mesh screen).
  • Component A comprises 55% of borosilicate glass (T s of about 820° C.) and 45% of a black pigment (Cr—Fe—Ni—Mn spinel), grain sizes of D50 ⁇ 5 ⁇ m, mixed with screen printing medium.
  • component A is baked at the same time and thereafter has a layer thickness of 1.4 ⁇ m, a smooth haptic perception, is dense, non-porous, gray, and semi-transparent.
  • component B1 is applied on component A by screen printing (77 mesh screen), likewise to the entire surface area thereof, and is dried at 200° C. for 90 min.
  • the resulting gradient layer including component A and component B1 is smooth, dense, and glossy black.
  • Component B1 is applied to the bottom surface of a transparent glass ceramic plate of the type CERAN CLEARTRANS® (size 250 ⁇ 300 mm, thickness 4 mm) over the entire surface thereof by screen printing (77 mesh screen) and is then dried at 200° C. for 90 min.
  • Component B1 obtained in this manner has a layer thickness of 20 ⁇ m and is dark gray black.
  • this plate is subjected to a thermal load of 500° C. it discolors (becomes lighter). Massive cracks are produced in the silicone layer, where the light is scattered more strongly.
  • the resulting color difference between the undamaged silicone layer and the silicone layer damaged by thermal action is not acceptable, i.e. the requirements for a cooktop are not met.
  • the material of component B1 is not suitable for a single layer coating.
  • Component A is applied to the bottom surface of a transparent glass ceramic plate of the type CERAN CLEARTRANS® (size 250 ⁇ 300 mm, thickness 4 mm) over the entire surface thereof by screen printing (140 mesh screen), and is baked at 725° C. for 10 min.
  • Component A comprises 40% of zinc borosilicate glass (T s of about 575° C.) and 30% of a blue pigment (Co—Al—Cr spinel) and 30% of a green pigment (Co—Zn—Ti—Cr spinel), grain sizes D50 ⁇ 5 ⁇ m.
  • Component A baked in this manner has a layer thickness of 2.1 ⁇ m, a smooth haptic perception, is dense and non-porous, turquoise, and semi-transparent.
  • component B2 which forms the further layer is applied on component A by screen printing, likewise to the entire surface area thereof.
  • a gray silicone paint is used as the component B2. This paint is printed using a 54 mesh screen, and is then dried at 230° C. for 45 min.
  • the resulting gradient layer consisting of component A and component B2 is smooth, opaque turquoise, and glossy.
  • the gradient layer so produced comprising the materials of component A and component B2 meets the requirements for a cooktop with a short-term temperature load of up to 500° C.
  • Component A is applied to the bottom surface of a heat-resistant borosilicate glass of the type Borofloat 33 of a thickness of 3 mm over the entire surface by screen printing (100-40 mesh screen).
  • Component A comprises 40% of bismuth-borosilicate glass (T s of about 600° C.) and 60% of a black pigment (Cu—Cr spinel). Baking is performed at 680° C. for 10 min. The resulting layer is almost black, dense, and has a layer thickness of 3.4 ⁇ m.
  • a black silicone paint is used as the component B1, for example that described in published patent application DE 10 2010 031 866 A1. This paint is printed using a 77 mesh screen, and is then dried at 200° C. for 45 min.
  • the resulting gradient layer including component A and component B1 is smooth, dense, and glossy black.
  • additional substrates were printed with the semi-transparent component A and baked. Then one half of the substrate was printed on the rear so as to become opaque (as described in the examples above), and the other half was printed on the rear with a transparent pigment-free silicone resin and then dried. Even with the transparent rear printing, the display below the plate is not visible in the off state, but when switched on the display is easy to read.
  • the transparent silicone resin was also colored with organic dyes, e.g. in Example 1 with black dye Orasol® RLi, or in Example 9 with phthalocyanine-based dyes.
  • the upper surface may also be decorated.
  • the invention enabled to provide a deep black coating of high temperature resistance, consisting of components A (first layer) and B (further layer).
  • the lightness L of the layer system consisting of components A and B is less than 27, whereas when applied alone component A has a lightness of 29.9 and component B has a lightness of 30.8.
  • component A has a lightness of 29.9
  • component B has a lightness of 30.8.
  • FIG. 2 shows a schematic flow chart of the essential method steps.
  • a glass ceramic substrate is provided, then a first layer is applied which consists of a layer material comprising metal oxide particles for pigmentation purposes and a glass flux material.
  • This first layer is baked at a temperature of more than 600° C., so that a dense textured layer is produced.
  • a black silicone paint is applied as a further layer. This silicone paint is dried at a temperature below 500° C.
  • FIG. 3 shows photographs of different samples of coated glass ceramic substrates.
  • Samples 6, 8, and 9 are coated glass ceramic substrates having a dark coating such as available on the market.
  • Sample 7 is coated using a noble metal oxide. As can be seen, it has a brown-black color appearance. However, the application of such a coating is very expensive.
  • Sample 5 has been coated using a method according to the invention.
  • the coating has a deep black color appearance. Furthermore, the coating has a glossy reflective color appearance.
  • FIG. 4 shows the spectral transmittance curve of a glass ceramic substrate coated with component A according to the embodiment of Example 1 of the invention.
  • FIG. 5 illustrates the lightness value (L value) in the Lab system of the samples shown in FIG. 3 .
  • sample 5 which is the coating applied according to the invention has the lowest L value, which is even lower than the L value of sample 7 in which a noble metal oxide was applied.
  • component A has a dark pigmentation.
  • FIGS. 7 to 10 show scanning electron micrographs of a glass flux based coating material for the first layer, which was baked at 680° C.
  • a highly textured layer can be seen, which due to the added particles has the desired high degree of texturing as intended.
  • FIG. 9 shows a micrographs with high magnification as compared to the scale illustrated in FIGS. 7 and 8 .
  • FIG. 10 shows a sectional view of the layer. It can be seen how the substrate merges into the coating, even the individual pigment particles are clearly visible. In the bottom of one valley, a significant cracking can be seen.
  • FIGS. 11 and 12 show scanning electron micrographs of a first layer with a pigment content of 70%, which was baked at 725° C. The result is roughly comparable, although the texture depth of this layer is further increased.
  • FIG. 12 illustrates particularly well that the layer is almost free of pores. Therefore, the layer material itself has a very low porosity after baking.
  • the first layer should be baked so fast that a formation of a porous structure due to the added particles is largely avoided.
  • FIGS. 13 and 14 show scanning electron microscope cross-sectional views of a layer material which has been filled with a silicone paint as the second layer.
  • FIG. 13 relates to the first layer with a pigment content of 65% baked at 680° C.
  • FIG. 14 relates to the first layer with a pigment content of 70% baked at 725° C.
  • the components of the first and the further layer are hardly distinguishable in this scanning micrograph, the material gradually merges into one another.
  • the invention permits, in a particularly simple and cost-effective manner, to produce high-temperature stable colored decorative coatings for cooktops.

Abstract

Glass or glass ceramic substrates are provided that have a decorative coating. Methods for coating a glass or glass ceramic substrate with a decorative coating are also provided. In the method, a first, textured layer is applied which is filled with a further layer, so that a layer material of graded composition is formed.

Description

CROSS REFERENCE TO RELATED APPLICATIONS
This application is a divisional of U.S. application Ser. No. 14/518,456 filed Oct. 20, 2014, which is a continuation of International Application PCT/EP2013/058224 filed Apr. 19, 2013, which claims benefit under 35 USC 119 of German Application 10 2012 103 507.5 filed Apr. 20, 2012 and German Application 10 2012 109 808.5 filed Oct. 15, 2012, the entire contents of all of which are incorporated herein by reference.
BACKGROUND 1. Field of the Invention
The invention relates to a method for producing a decorative coating on a glass or glass ceramic substrate and to a glass or glass ceramic substrate produced according to such method. More particularly, the invention relates to a glass ceramic cooktop having a bottom surface coating.
2. Description of Related Art
Glass and glass ceramic substrates with a decorative coating are known from practice. A problem with such coatings is that the layer system is subjected to high thermal loads. When used for induction cooktops, for example, the coatings have to resist temperatures of up to 500° C.
A variety of ways for applying such coatings have already been known from practice.
First, it is known to deposit metallic layers using a PVD process, these layers may in particular be applied by sputtering. Sputtered layers are highly brilliant and have a metallic appearance.
A drawback, however, is that sputtering of metallic layers is quite complex. In particular if it is desired to only partially cover the substrate with a decorative layer, for example in order to mark cooking zones, additional process steps for masking are necessary.
Another drawback is due to the fact that there are only few possibilities to vary the visual appearance of the coating, in particular in terms of the desired color. For example it is very complex to apply black layers using a sputtering process.
Often, another drawback is the conductivity of the layers, which usually makes them not suitable to be arranged in front of capacitive switches.
Also known from practice are decorative coatings based on silicone paints. Although the latter may be applied comparatively easily by screen printing, the mechanical strength of such layers, however, is usually limited, and moreover, discoloration of the coating may be caused under high temperature loads.
Furthermore, it is known to apply decorative coatings by means of glass flux, i.e. enamel coatings. Such enamel coatings have the advantage that by selecting the employed pigments which are added to the glass flux material almost any color can be produced.
However, known glass flux-based coatings can usually only be applied in a limited layer thickness with the resulting opacity and are prone to cracking, which has a significant impact on the visual appearance of the layer. Furthermore, known enamel layers put the employed substrate under tension thus reducing its strength.
In order to prevent cracking and to improve the mechanical strength of the composite material produced, it is known to apply porous enamel layers. However, a drawback of these layers is that the pores are in the range of the wavelength of visible light, so that a matt appearance is caused.
EP 1 435 759 B1 describes a method for applying a decorative coating onto a cooktop, in which a dense layer containing inorganic pigments is applied to the upper surface and a porous layer containing inorganic pigments to the bottom surface. The intention therein is to avoid cracks in the bottom layer by all means.
Mechanically and thermally stable glossy enamel layers for cooktops could not be produced so far.
Also known are coatings produced by a sol-gel process in which at least one pigment or filler is added to the sol-gel material. However, in many cases such sol-gel layers are also prone to delamination or cracking, which is then manifested as a local lightening on the composite material.
Furthermore, it is known to apply luster paints as a decorative coating. A drawback with luster paints, again, is that the selection of the color location is limited and that at least for dark, especially for black coatings noble metal based paints have to be used, which involves increased manufacturing costs.
SUMMARY
The invention is based on the object to provide a method for applying a decorative coating to glass or ceramic substrates, which permits to easily provide the substrate with a heat-resistant layer.
A more particular object of the invention is to provide for free selection of the color location of the coating and for application of a glossy layer.
The object of the invention is already achieved by a method for applying a decorative coating to a glass or glass ceramic substrate and by a coated glass or glass ceramic substrate.
The invention relates to a method for applying a decorative coating to a glass or glass ceramic substrate.
A decorative coating refers to any coating that changes the visual appearance of the substrate. Preferably, the coating is opaque or semi-transparent. The coating may be of any desired color.
Preferably, a transparent and/or heat-resistant material is used as the glass or glass ceramic substrate. Besides glass ceramics which are known as so-called zero-expansion material, it is also conceivable for the invention to be employed for heat-resistant glasses. However, in the case of a cooktop application a glass ceramic substrate will usually be used. A transparent substrate refers to a substrate which is at least partially transparent in the visible range.
The substrate is preferably planar. However, it is also conceivable to use the invention for curved substrates, e.g. those used for fireplace windows.
According to the invention, a first layer having a textured surface is initially applied using a glass flux. A textured surface refers to a surface that has a surface relief. That means, the applied coating is not flat but has valleys and mountains. The texture depth is preferably in the micrometer range. In particular, a maximum texture depth from 0.1 to 5 μm, preferably from 0.2 to 3 μm, and more preferably from 0.5 to 2 μm is contemplated.
The texture depth may be determined, for example, by measuring the surface profile of a sample material along 10 randomly selected test sections of a length of 1 cm, for example by scanning electron microscopy.
The average value of the 10 maximum height differences so determined represents the maximum texture depth for the purposes of the invention.
Such a textured surface is achieved by adding pigment and/or filler particles to the material employed for the coating, as will be explained in more detail below.
A further layer is applied onto the textured first layer, which at least partially and more preferably completely fills the textured surface, so that the material of the first layer gradually merges into the material of the second layer. It is also conceivable to fill the first layer with the layer material of the second layer only in sections of the first layer.
Since the produced mountain-valley profile is filled by the material of the second layer, the material composition of the layer system comprised of the two materials changes, starting from the substrate up to the surface of the coating, in that a higher proportion of the material of the first layer is present at the surface of the substrate (preferably approximately 100%), whereas on the surface of the layer system the proportion of the material of the first layer is smaller (preferably approximately 0%).
The inventors have found that under thermal load the resulting layer system is much less prone to clearly visible changes, in particular to light stains caused by cracking.
This may be due to the fact that even if cracks are produced in the first layer, these will usually be concealed by the second layer, so that despite of existing cracking the inhomogeneities in visual appearance mentioned above do not occur.
Moreover, intended cracking may even cause a generation of zones of increased temperature resistance, which results in enhance temperature resistance of the entire layer system. This is especially true in case of a first layer produced by glass flux onto which a polymer layer is applied.
It will be understood that further layers may be present within the meaning of the invention. In particular, further covering and sealing layers are conceivable.
Also, as contemplated according to a further embodiment of the invention, it is possible for the layer system consisting of the first and the further layer to be applied onto a layer having a high texture depth of several microns. This may in particular be a layer deposited by a sol-gel process. By using such a further textured layer of high textural depth of preferably more than 10 μm, it is possible to produce patterns, haptic grip surfaces etc., for example. These may in particular be arranged on the bottom surface of a substrate, in particular of a cooktop.
Preferably, the material of the first and/or second layer comprises pigments, in particular in a proportion of more than 50% (% values always given in percent by weight, unless otherwise indicated).
In particular the layer used as the first layer preferably has a high pigment content of more than 60%.
Preferably metal oxides are used as the pigments. These may in particular include: cobalt oxides/spinels, cobalt-aluminum spinels, cobalt-titanium spinels, cobalt-chromium spinels, cobalt-nickel-manganese-iron-chromium oxides/spinels, cobalt-nickel-zinc-titanium-aluminum oxides/spinels, iron oxides, iron-chromium oxides, iron-chromium-zinc-titanium oxide, copper-chromium spinels, nickel-chromium-antimony-titanium oxides, titanium oxides, zirconium-silicon-iron oxides/spinels etc.
Moreover, any conceivable absorption pigments are also eligible as the pigments, in particular platelet- or rod-shaped pigments. It is also possible to use coated effect pigments.
Furthermore, it is possible to add fillers in particular to the first layer, which fillers may especially include: SiO2 particles, alumina particles, fumed silica, soda-lime, alkali-aluminosilicate or borosilicate glass spheres, hollow glass spheres.
In combination with a high percentage of pigment particles and/or fillers, a layer with a high texture depth will be formed.
Preferably, the layer is baked at such a high temperature that the glass flux particles melt while the filler and/or pigment particles substantially remain intact, so as to obtain a dense layer having a high texture depth.
A dense layer in particular refers to a layer having a closed porosity of less than 5%.
In this way, in particular a semi-transparent rough first layer is formed, which is filled with a polymer layer as the further layer in order to provide, in combination, an opaque glossy bottom surface coating.
It is also conceivable to omit the further layer in sections in order to obtain a semi-transparent surface area in the omitted area. This semi-transparent area may in particular serve for integrating a display. In particular the use of a screen printing process for applying the further layer permits to easily produce the recessed areas.
It will be understood that the recessed area may yet contain further, third layer materials.
For example it is conceivable to apply a transparent polymer layer onto the first layer in the recessed area. Also, it is conceivable to apply a semi-transparent layer that contains other colorants than the recessed further layer. So the omitted area remains semi-transparent and may be adapted to the adjacent layer system in terms of its visual appearance.
The layer thickness of the first layer is preferably between 0.1 and 10 μm, more preferably between 1 and 5 μm. The further layer preferably has a thickness from 1 μm to 100 μm.
The maximum texture depth of the first layer is preferably more than 40%, more preferably more than 80%, and most preferably more than 90% of the maximum layer thickness.
As a glass flux material of the first layer, crystalline or glassy inorganic materials may be used.
The glass flux material is preferably provided in particulate form and is optionally mixed with the pigment and/or filler particles.
The glasses preferably used are silicate glasses such as borosilicate glasses, zinc-borosilicate glasses, bismuth-borosilicate glasses, silicon oxide glasses, zinc-silicate glasses, bismuth-silicate glasses, aluminosilicate glasses, invert glasses, or borate and phosphate glasses, such as zinc-borate glasses, bismuth-borate glasses.
The first layer is preferably baked at a temperature of more than 500° C., most preferably of more than 600° C.
“Baking” in the meaning of the invention refers to curing of the coating material. In the case of a glass flux, the material is in particular baked at such a high temperature that the glass flux material melts and does not only sinter.
The heating is preferably performed so rapidly and temporarily that the glass flux material densifies without bringing about any evaporation processes to occur, which might cause pore formation. However, the glass flux material has to be that fluid that it completely wets the settled pigment particles and/or fillers.
The layer material used for the further layer is preferably a polymer. In particular a polysiloxane, polysilsesquioxane, polyurethane, epoxy- and/or polyester-functionalized silicone resins, or a sol-gel may be used.
Preferably, the further layer is also mixed with pigments, in particular inorganic pigments and/or fillers and/or organic colorants.
The fillers used include in particular silica particles, alumina particles, fumed silica, soda-lime, alkali-alumosilicate or borosilicate glass spheres, hollow glass spheres.
Pigments that come into consideration include any conceivable absorption pigments, in particular platelet- or rod-shaped pigments.
It is also conceivable to use coated effect pigments.
Colorants that may be used include any organic colorants which are sufficiently temperature stable.
In particular for the display area, transparent layer material may be used for the second layer, which may however even be colorized in order to reduce the color contrast between the opaque part and the display area. For coloring the layer, various coloring agents may be used which provide a semi-transparent coating with low scattering.
For example organic colorants may be added to the coating material. For a dark or black coating, in particular Orasol® RLi may be used. Temperature resistant colorants that are also suitable include azo dyes such as methyl orange, alizarin yellow or Congo red; triphenylmethane dyes such as malachite green, eosin, fluorescein, aurin, and phenolphthalein; Vat dyes such as anthraquinone dyes, indigo, and thioindigo; fluorescent dyes; perylene dyes.
Also, phthalocyanines with e.g. Cr, Cu, Ni, Zn, or Co as the central atom may be employed.
Through the use of a polymeric layer which by filling up the texture of the first layer forms a layer system of a graded composition, a dense, optionally glossy, thermally highly resistant layer system is obtained. This resulting gradient layer has a porosity of less than 7 vol % and is thus dense. This value can be determined in a cross section. Nitrogen sorption according to BET reveals surface areas of the layer system of less than 5 m2/g, which again is evidence of a dense gradient composite.
The invention in particular permits in a very simple way to produce black glossy layers of high thermal resistance. The layers are in particular resistant to a short-term temperature load of more than 500° C. and to a long-term exposure to more than 400° C.
Surprisingly, black layers can be produced by combining a first and a further layer, which when individually applied each have a lightness L in the Lab color space of more than 29.0. That means, these layers are rather gray and do not exhibit the desired black color appearance.
Surprisingly, a combination of these layers results in a lightness L of less than 28.0, in particular less than 27.0.
Heretofore, high cost noble metal oxides were necessary to provide such dark heat-resistant layers which, in addition, had a slightly brownish color deviation.
The application of the layer material of the first and/or further layer is preferably accomplished using a printing technique, in particular by screen printing.
In this manner, even large area substrates can be completely coated very easily and rapidly.
At the same time, the use of a screen printing process permits to only partially coat the substrate. That means, it is possible to print only certain areas while other areas are left out. In case of a cooktop, in particular the display areas or the hobs may be left out.
Moreover, even combinations of multi-colored top and bottom coatings are possible.
The invention further relates to a coated glass or glass ceramic substrate which can be produced as described above.
With the invention it was possible to provide a glossy coating which in particular shines with a gloss level of G1 according to EN ISO 2813. It will be understood that for the bottom surface coating the gloss level considered is that as seen from the side of the substrate.
BRIEF DESCRIPTION OF THE DRAWINGS
The patent or application file contains at least one drawing executed as a photograph. Copies of this patent or patent application publication with the photographs(s) will be provided by the Office upon request and payment of the necessary fee.
FIG. 1 is a schematic cross-sectional view of the glass or glass ceramic of the present disclosure.
FIG. 2 shows a schematic flow chart of the essential method steps.
FIG. 3 shows photographs of different samples of coated glass ceramic substrates according to the present disclosure.
FIG. 4 shows the spectral transmittance curve of a glass ceramic substrate coated with component A according to the embodiment of Example 1 of the invention.
FIG. 5 illustrates the lightness value (L value) in the Lab system of the samples shown in FIG. 3 .
FIG. 6 illustrates the change in color location due to rear printing with different colors.
FIG. 7 shows a scanning electron micrograph, from a top view, of a glass flux based coating material for the first layer which was baked at 680° C. at 1,000 times magnification.
FIG. 8 shows a scanning electron micrograph, from the top view, of the glass flux based coating material of FIG. 7 at 5,000 times magnification.
FIG. 9 shows a scanning electron micrograph, from the top view, of the glass flux based coating material of FIG. 7 at 100,000 times magnification.
FIG. 10 shows a scanning electron micrograph, from a sectional view, of the glass flux based coating material of FIG. 7 at 50,000 times magnification.
FIG. 11 shows a scanning electron micrograph, from a top view, of a first layer with a pigment content of 70%, which was baked at 725° C. at 20,000 times magnification.
FIG. 12 shows a scanning electron micrograph, from a sectional view, of the first layer of FIG. 11 at 50,000 times magnification.
FIG. 13 shows a scanning electron microscope cross-sectional view of a first layer with a pigment content of 65% baked at 680° C. at 10,000 times magnification.
FIG. 14 shows a scanning electron microscope cross-sectional view of a first layer with a pigment content of 70% baked at 725° C. at 10,000 times magnification.
DETAILED DESCRIPTION
The invention will now be described with reference to the drawings of FIGS. 1 to 14 .
FIG. 1 is a schematic cross-sectional view which serves to illustrate the effect of the invention.
A coated glass or glass ceramic substrate 1 can be seen which consists of the substrate 2 and a gradient layer.
The gradient layer comprises a first layer 3 applied using a glass flux, which layer contains more than 60% of pigment particles and small filler particles.
Due to the presence of the pigment particles which form randomly distributed valleys and mountains, a textured surface is formed which is filled with a polysiloxane layer as a further layer 4. The further layer 4 also contains pigment particles. The gradient layer is used as a bottom surface coating, that means the viewer will look at the gradient layer from the side opposite layers 3 and 4.
The gradient layer is preferably black and glossy.
In more detail, layers may be applied as described in the examples below.
The layer material used for the first layer has a composition according to component A, and the further layer has a composition according to component B.
For the matrix material of component A, in particular crystalline and/or glassy inorganic materials can be used.
Preferably, these basic glasses may be of siliceous origin, such as e.g. borosilicate glasses, fused silica glasses, zinc-silicate glasses, zinc-borosilicate glasses, bismuth-silicate glasses, bismuth-borosilicate glasses, alumosilicate glasses, soda-lime glasses, or borate, zinc-borate, bismuth-borate glasses, or phosphate glasses, and invert glasses.
These may include, for example, glasses of the following composition:
Borosilicate Glass:
    • SiO2: 45-85 wt %
    • B2O3: 5-30 wt %
    • Al2O3: 2-20 wt %
    • R2O: 2-20 wt, R2O representing alkali oxides
    • RO: 0-10 wt %, RO representing alkaline earth oxides
    • RO2: 0-5 wt %, RO2 representing TiO2 and/or ZrO2
    • ZnO: 0-15 wt %.
Zinc-Borate Glasses:
    • SiO2: 10-45 wt %
    • B2O3: 5-30 wt %
    • Al2O3: 0-10 wt %
    • R2O: 0-10 wt %, R2O representing alkali oxides
    • RO: 0-25 wt %, RO representing alkaline earth oxides
    • RO2: 0-10 wt %, RO2 representing TiO2 and/or ZrO2
    • ZnO: 10-70 wt %.
A coated glass or glass-ceramic substrate may be produced in detail with reference to the following examples:
Example 1
Component A is applied to the bottom surface of a transparent glass ceramic plate of the type CERAN CLEARTRANS® (size 250×300 mm, thickness 4 mm) over the entire surface by screen printing (180 mesh screen), and is baked at 725° C. for 10 min in a continuous furnace. Component A comprises 35% of zinc-borosilicate glass (softening point Ts of 575° C.) and 65% of a black pigment (Cu—Cr spinel; CuCr2O4), both components having a grain size of D50<5 μm.
Component A baked in this manner has a layer thickness of 1.8 μm, a smooth haptic perception, is dense and non-porous (a dried water droplet can be wiped off), is gray (results of color measuring device Datacolor: L=29.9; a=−0.4; b=0.4), and semi-transparent (transmittance at 550 nm: 11%).
In order to determine the scattering of the layer, a sample was measured in a spectrometer “Lambda 900” from company Perkin Ellmer, with and without Ulbricht sphere. At a wavelength of 550 nm, the transmittance was 11% with Ulbricht sphere and 1% without sphere, which means the sample exhibits a high level of scattered light.
Subsequently, component B1 which forms the further layer is applied on component A by screen printing, also to the entire surface area.
A black silicone paint is used as the component B1, for example that described in published patent application DE 10 2010 031 866 A1. This paint is printed using a 77 mesh screen, and is then dried at 200° C. for 45 min.
The resulting component B1 has a layer thickness of 11 μm and is gray when printed alone (L=30.8; a=−0.25; b=−1.2).
The gradient layer resulting from component A and component B1, however, is smooth, dense, deep black (L=26.7; a=−0.1; b=−0.7) and glossy when viewed through the glass ceramic (i.e. viewed from the upper side); transmittance in the entire visible range is 0% (transmission measurement with and without Ulbricht sphere). The spectrometer “Lambda 950” from company Perkin Ellmer was used to measure both the individual layer of component A and the gradient layer including components A and B1 in reflection. The difference in haze values is 5.5%, that means the reflection measurements confirmed that the layer consisting of component A has a high scattering power, while the gradient composite exhibits almost no scattering behavior.
The gradient layer so produced, consisting of the materials of components A and B, meets the requirements for a cooktop with a short-term temperature load of up to 500° C.
In detail, component B1 may have a composition as follows:
    • 60-80 wt % polydimethylsiloxane
    • 10-40 wt % black pigment, in particular selected from the group comprising (Cr,Fe)(Ni,Mn) spinel; Cu(Cr,Fe,Mn)2O4 spinel (black 28); Co(Cr,Fe)2O4 (black 27); (Ni,Fe)(Cr,Fe)O4 spinel (black 30); (Fe,Mn)2O3 (black 33); (Fe,Mn)(Fe,Mn)2O4 spinel (black 26); and (Cu,Cr)Ox (black 28)
    • 5-15 wt % graphite with a D90 value between 5 and 20 μm. (both synthetic and non-synthetic).
Example 2
Component A is applied to the bottom surface of a transparent glass ceramic plate of the type CERAN CLEARTRANS® (size 250×300 mm, thickness 4 mm) over the entire surface by screen printing and is baked in a continuous furnace at 750° C. for 15 min.
Component A comprises 25% of borosilicate glass (Ts of about 620° C.) and 75% of black pigment (Cu—Cr spinel), with grain sizes of D50<5 μm.
Component A baked in this manner has a layer thickness of 1.6 μm, a smooth haptic perception, is dense (non-porous), dark gray (L=30.8; a=−0.4; b=0.2) and semi-transparent.
Subsequently, component B2 is applied on component A by screen printing (77 mesh screen), likewise to the entire surface area, and is dried at 230° C. for 90 min. A gray silicone paint is used as the component B2. The resulting gradient layer including component A and component B2 is smooth, dense, opaque, and dark gray (L=30.1; a=−0.7; b=−0.8).
The so produced plate with the gradient layer satisfies the requirements for a cooktop with a short-term temperature load of up to 500° C.
In detail, component B2 may have a composition as follows:
    • 60-80 wt % polydimethylsiloxane
    • 10-20 wt % black pigment, in particular selected from the group comprising (Cr,Fe)(Ni,Mn) spinel; Cu(Cr,Fe,Mn)2O4 spinel (black 28); Co(Cr,Fe)2O4 (black 27); (Ni,Fe)(Cr,Fe)O4 spinel (black 30); (Fe,Mn)2O3 (black 33); (Fe,Mn)(Fe,Mn)2O4 spinel (black 26); and (Cu,Cr)Ox (black 28)
    • 10-20 wt % TiO2 (white pigment)
    • 5-15 wt % graphite with a D90 value between 5 and 20 μm. (both synthetic and non-synthetic).
Example 3
Component A is applied to the bottom surface of a transparent glass ceramic plate of the type CERAN CLEARTRANS® (size 250×300 mm, thickness 4 mm) over the entire surface by screen printing (180 mesh screen) and is then dried.
Component A comprises 90% of borosilicate glass (Ts of about 755° C.) and 10% of an effect pigment (Merck, type Xirallic®—crystal silver), mixed with screen printing medium.
Subsequently, component B is applied onto component A by screen printing (140 mesh screen), also to the entire surface area, and is dried at 825° C. for 10 min.
Component B comprises 30% of zinc-borosilicate glass (Ts of about 575° C.) and 70% of a black pigment (Fe—Ni—Cr spinel), grain sizes D50<5 μm.
A black silicone paint as described in Example 1 is used as a component C(=B1).
This paint is printed using a 77 mesh screen, and is then dried at 230° C. for 45 min. The resulting gradient layer including components A, B, and C is smooth, dense, and, when viewed from the upper side, black with glitter effect.
Component A may also be produced using borosilicate glasses of different composition with varying contents of effect pigments (e.g. 1-10%). In this way, the visual appearance may be changed, e.g. as black with gold glitter or black with stainless steel color glitter.
The gradient layers so produced satisfy the requirements for a cooktop with a short-term temperature load of up to 500° C.
Example 4
A sol-gel paint (preparation described in published patent application WO2010/081531 A1) including 25% of effect pigment (Merck, type Iriodin®; particle size <25 μm) is applied to the bottom surface of a transparent glass ceramic plate of the type CERAN CLEARTRANS® (size 250×300 mm, thickness 4 mm) over the entire surface thereof by screen printing, 140 mesh screen, in form of geometric patterns and labeling, and is dried at 150° C. for 10 min to obtain a layer thickness of 8 μm. Subsequently, the gradient layer is produced in the manner as described in Example 1.
The resulting plates are deep black (L=26.6; a=−0.2; b=−0.7) when viewed from the upper side (viewer side), with bright contrasting patterns, markings and lettering (L=63; a=−1.7; b=2.1).
The plates thus produced meet the requirements for a cooktop with a short-term temperature load of up to 500° C.
Example 5
Component A is applied to the bottom surface of a plurality of transparent glass ceramic plates of the type CERAN CLEARTRANS® (size 250×300 mm, thickness 4 mm) over the entire surface by screen printing (100 mesh screen), and is baked at 725° C. for 10 min.
Component A comprises 35% of zinc-borosilicate glass (Ts of about 575° C.) and 65% of a white pigment (TiO2), with grain sizes of D50<5 μm.
Component A baked in this manner has a layer thickness of 3 μm, a smooth haptic perception, is dense (non-porous), beige (L=63.69; a=−0.3; b=5.61) and semi-transparent.
Subsequently, components B1, B2, and B3 are applied to different plates over component A by screen printing, likewise to the entire surface area thereof and using a 77 mesh screen, and then are dried at 200° C. for 45 min.
The resulting plate with the gradient layer including component A and component B1 is smooth, dense, and gray (L=48; a=−2; b=−3) when viewed from the upper side; the resulting plate with the gradient layer including component A and component B2 is smooth, dense, and light gray (beige gray) (L=59; a=−1.6; b=1.4). The resulting plate with the gradient layer including component A and component B3 is smooth, dense, and beige (significantly more opaque (less transparent) than component A alone) (L=69; a=−0.7; b=5.5). The plates with the gradient layers so produced satisfy the requirements for a cooktop with a short-term temperature load of up to 500° C.
In detail, component B3 may have a composition as follows:
    • 60-80 wt % of polydimethylsiloxane
    • 0-40 wt % of TiO2 (white pigment)
    • 0-10 wt % of effect pigment iriodin.
Example 6
Component A is applied to the bottom surface of a transparent glass ceramic plate of the type CERAN CLEARTRANS® (size 250×300 mm, thickness 4 mm) over the entire surface thereof by screen printing, and is baked at 800° C. for 30 min.
Component A comprises 70% of borosilicate glass (Ts of about 820° C.) and 30% of a black pigment (Cr—Fe—Ni—Mn spinel), grain sizes of D50<5 μm.
Component A baked in this manner has a layer thickness of 4.2 μm, a smooth haptic perception, is dense, non-porous, gray (L=33.1; a=−1; b=−0.9) and semi-transparent. Subsequently, component B1 is applied on component A by screen printing (77 mesh screen), likewise to the entire surface area thereof, and is dried at 200° C. for 90 min. The resulting gradient layer including component A and component B1 is smooth, dense, black (L=27.5; a=−0.2; b=−0.9) and glossy.
It may occur that a bead of adhesive which is applied to the bottom surface, is visible from the upper side. Therefore, it is also possible to first apply component A of Example 1 and then the layers according to Example 6.
Example 7
Component A is applied to the bottom surface of a transparent, non-ceramized glass plate of the type CERAN CLEARTRANS® (size 250×300 mm, thickness 4 mm) over the entire surface thereof by screen printing (180 mesh screen). Component A comprises 55% of borosilicate glass (Ts of about 820° C.) and 45% of a black pigment (Cr—Fe—Ni—Mn spinel), grain sizes of D50<5 μm, mixed with screen printing medium.
During ceramization of the substrate, component A is baked at the same time and thereafter has a layer thickness of 1.4 μm, a smooth haptic perception, is dense, non-porous, gray, and semi-transparent.
Subsequently, component B1 is applied on component A by screen printing (77 mesh screen), likewise to the entire surface area thereof, and is dried at 200° C. for 90 min. The resulting gradient layer including component A and component B1 is smooth, dense, and glossy black.
Example 8 (Comparative Example)
Component B1 is applied to the bottom surface of a transparent glass ceramic plate of the type CERAN CLEARTRANS® (size 250×300 mm, thickness 4 mm) over the entire surface thereof by screen printing (77 mesh screen) and is then dried at 200° C. for 90 min. Component B1 obtained in this manner has a layer thickness of 20 μm and is dark gray black. When this plate is subjected to a thermal load of 500° C. it discolors (becomes lighter). Massive cracks are produced in the silicone layer, where the light is scattered more strongly. The resulting color difference between the undamaged silicone layer and the silicone layer damaged by thermal action is not acceptable, i.e. the requirements for a cooktop are not met. Hence, the material of component B1 is not suitable for a single layer coating.
Example 9
Component A is applied to the bottom surface of a transparent glass ceramic plate of the type CERAN CLEARTRANS® (size 250×300 mm, thickness 4 mm) over the entire surface thereof by screen printing (140 mesh screen), and is baked at 725° C. for 10 min. Component A comprises 40% of zinc borosilicate glass (Ts of about 575° C.) and 30% of a blue pigment (Co—Al—Cr spinel) and 30% of a green pigment (Co—Zn—Ti—Cr spinel), grain sizes D50<5 μm.
Component A baked in this manner has a layer thickness of 2.1 μm, a smooth haptic perception, is dense and non-porous, turquoise, and semi-transparent.
Subsequently, component B2 which forms the further layer is applied on component A by screen printing, likewise to the entire surface area thereof.
A gray silicone paint is used as the component B2. This paint is printed using a 54 mesh screen, and is then dried at 230° C. for 45 min.
The resulting gradient layer consisting of component A and component B2 is smooth, opaque turquoise, and glossy.
The gradient layer so produced comprising the materials of component A and component B2 meets the requirements for a cooktop with a short-term temperature load of up to 500° C.
Example 10
Component A is applied to the bottom surface of a heat-resistant borosilicate glass of the type Borofloat 33 of a thickness of 3 mm over the entire surface by screen printing (100-40 mesh screen). Component A comprises 40% of bismuth-borosilicate glass (Ts of about 600° C.) and 60% of a black pigment (Cu—Cr spinel). Baking is performed at 680° C. for 10 min. The resulting layer is almost black, dense, and has a layer thickness of 3.4 μm.
A black silicone paint is used as the component B1, for example that described in published patent application DE 10 2010 031 866 A1. This paint is printed using a 77 mesh screen, and is then dried at 200° C. for 45 min.
The resulting gradient layer including component A and component B1 is smooth, dense, and glossy black.
Example 11
In the examples mentioned, additional substrates were printed with the semi-transparent component A and baked. Then one half of the substrate was printed on the rear so as to become opaque (as described in the examples above), and the other half was printed on the rear with a transparent pigment-free silicone resin and then dried. Even with the transparent rear printing, the display below the plate is not visible in the off state, but when switched on the display is easy to read. In order to keep the color contrast as small as possible between the opaque part and the semi-transparent display area, the transparent silicone resin was also colored with organic dyes, e.g. in Example 1 with black dye Orasol® RLi, or in Example 9 with phthalocyanine-based dyes.
Further Optional Embodiments
For cooktop applications, for example, in addition to the bottom surface the upper surface may also be decorated.
The invention enabled to provide a deep black coating of high temperature resistance, consisting of components A (first layer) and B (further layer).
Layers were in particular provided with the following color values in the Lab color space:
Layer L a B
Component A 29.9 −0.4 0.4
Component B 30.8 −0.25 −1.2
A + B 26.7 −0.1 −0.7
It is in particular apparent that the lightness L of the layer system consisting of components A and B is less than 27, whereas when applied alone component A has a lightness of 29.9 and component B has a lightness of 30.8. Thus, only a combination of the two components that make up the first layer and the further layer results in a deep black color appearance.
FIG. 2 shows a schematic flow chart of the essential method steps.
First, a glass ceramic substrate is provided, then a first layer is applied which consists of a layer material comprising metal oxide particles for pigmentation purposes and a glass flux material.
This first layer is baked at a temperature of more than 600° C., so that a dense textured layer is produced.
Then, a black silicone paint is applied as a further layer. This silicone paint is dried at a temperature below 500° C.
FIG. 3 shows photographs of different samples of coated glass ceramic substrates. Samples 6, 8, and 9 are coated glass ceramic substrates having a dark coating such as available on the market.
It can be seen that the visual appearance is rather greyish.
Sample 7 is coated using a noble metal oxide. As can be seen, it has a brown-black color appearance. However, the application of such a coating is very expensive.
Sample 5 has been coated using a method according to the invention.
As can be seen, it has a deep black color appearance. Furthermore, the coating has a glossy reflective color appearance.
FIG. 4 shows the spectral transmittance curve of a glass ceramic substrate coated with component A according to the embodiment of Example 1 of the invention.
It can be seen that in the visible range spectral transmittance is less than 20%.
FIG. 5 illustrates the lightness value (L value) in the Lab system of the samples shown in FIG. 3 .
It can be seen that sample 5 which is the coating applied according to the invention has the lowest L value, which is even lower than the L value of sample 7 in which a noble metal oxide was applied.
Referring to FIG. 6 , the change in color location due to rear printing with different colors will be explained.
In this example, component A has a dark pigmentation.
It can be seen that when used as a bottom surface coating (front view) a gray color appearance is obtained together with light pigmented component B2.
FIGS. 7 to 10 show scanning electron micrographs of a glass flux based coating material for the first layer, which was baked at 680° C.
A highly textured layer can be seen, which due to the added particles has the desired high degree of texturing as intended.
FIG. 9 shows a micrographs with high magnification as compared to the scale illustrated in FIGS. 7 and 8 .
In FIG. 9 cracking in the baked layer can be seen. Surprisingly it has been found that this cracking has no significant visible impact on the visual appearance of the layer when the latter is combined with a further layer which fills the texture of the first layer.
Moreover, cracking even appears to increase the temperature stability of the coating system.
FIG. 10 shows a sectional view of the layer. It can be seen how the substrate merges into the coating, even the individual pigment particles are clearly visible. In the bottom of one valley, a significant cracking can be seen.
FIGS. 11 and 12 show scanning electron micrographs of a first layer with a pigment content of 70%, which was baked at 725° C. The result is roughly comparable, although the texture depth of this layer is further increased.
The sectional view of FIG. 12 illustrates particularly well that the layer is almost free of pores. Therefore, the layer material itself has a very low porosity after baking.
The first layer should be baked so fast that a formation of a porous structure due to the added particles is largely avoided.
FIGS. 13 and 14 show scanning electron microscope cross-sectional views of a layer material which has been filled with a silicone paint as the second layer.
Here, FIG. 13 relates to the first layer with a pigment content of 65% baked at 680° C., and FIG. 14 relates to the first layer with a pigment content of 70% baked at 725° C.
It can be seen in the scanning electron micrographs that the first layer is sealed and a fairly smooth surface is obtained.
Furthermore, the components of the first and the further layer are hardly distinguishable in this scanning micrograph, the material gradually merges into one another.
The invention permits, in a particularly simple and cost-effective manner, to produce high-temperature stable colored decorative coatings for cooktops.

Claims (24)

What is claimed is:
1. A coated glass ceramic substrate, comprising:
a substrate made of glass ceramic having a top surface and a bottom surface, the top surface being configured as a cooktop;
a first layer on the bottom surface of the substrate, the first layer including pigment particles embedded in a glass flux, the first layer having a textured surface that has a maximum texture depth from 0.1 to 5 μm that is more than 40% of a maximum thickness of the first layer; and
a second layer on the first layer, the second layer at least partially filling the textured surface of the first layer so that the second layer is merged into the first layer with components of the first and second layers being hardly distinguishable from one another in a scanning micrograph,
wherein the first layer comprises pigments in a proportion of more than 50% by weight.
2. The coated glass ceramic substrate of claim 1, wherein the second layer is a polymeric layer.
3. The coated glass ceramic substrate of claim 2, wherein the polymeric layer includes colorants or pigments.
4. The coated glass ceramic substrate of claim 1, wherein the first and second layers form a gradient layer that is black.
5. The coated glass ceramic substrate of claim 1, wherein the second layer is selected from a group consisting of a polysiloxane, polysilsesquioxane, polyurethane, epoxy-functionalized silicone resin, polyester-functionalized silicone resin, and a sol-gel.
6. The coated glass ceramic substrate of claim 1, wherein the second layer comprises pigments in a proportion of more than 50% by weight.
7. The coated glass ceramic substrate of claim 6, wherein the pigment particles of the first layer comprise metal oxide particles, and wherein the first layer further comprises an inorganic material.
8. The coated glass ceramic substrate of claim 1, wherein the pigment particles of the first layer have a mean particle size of more than 0.25 μm.
9. The coated glass ceramic substrate of claim 1, wherein the first and second layers individually exhibit a lightness L in the Lab color space of more than 29.0, and wherein the first and second layers combined exhibit a lightness L of less than 28.0.
10. The coated glass ceramic substrate of claim 1, further comprising a further textured layer below the first layer.
11. The coated glass ceramic substrate of claim 10, wherein the further textured layer is omitted in at least one area.
12. The coated glass ceramic substrate of claim 1, wherein the first layer further comprises filler particles.
13. The coated glass ceramic substrate of claim 1, wherein the first layer has a closed porosity of less than 30%.
14. The coated glass ceramic substrate of claim 1, wherein the second layer has a gloss level of G1 according to EN ISO 2813 when viewed through the substrate from a side opposite the first and second layers.
15. A cooktop comprising the coated glass ceramic substrate of claim 1.
16. The cooktop of claim 15, comprising a display area and/or a hob, wherein the first and second layers are left out of the display area and/or the hob.
17. The coated glass ceramic substrate of claim 1, wherein the textured surface further comprises cracks, wherein the second layer at least partially fills the textured surface and the cracks so that the second layer is merged into the first layer.
18. The substrate of claim 1, wherein the substrate is made of a zero-expansion material.
19. A coated glass ceramic substrate, comprising:
a substrate made of glass ceramic having a top surface and a bottom surface, the top surface being configured as a cooktop;
a first layer on the bottom surface the substrate, the first layer including pigment particles embedded in a glass flux, the first layer having a textured surface that has a maximum texture depth from 0.1 to 5 μm that is more than 40% of a maximum thickness of the first layer; and
a second layer on the first layer, the second layer at least partially filling the textured surface of the first layer so that the second layer is merged into the first layer with components of the first and second layers being hardly distinguishable from one another in a scanning micrograph, wherein the second layer is selected from a group consisting of a polysiloxane, polysilsesquioxane, polyurethane, epoxy-functionalized silicone resin, and polyester-functionalized silicone resin, wherein the first layer comprises pigments in a proportion of more than 50% by weight.
20. The substrate of claim 19, wherein the substrate is made of a zero-expansion material.
21. A coated glass ceramic substrate, comprising:
a substrate made of glass ceramic having a top surface and a bottom surface, the top surface being configured as a cooktop;
a first layer on the bottom the substrate, the first layer including pigment particles embedded in a glass flux, the first layer having a textured surface comprising cracks; and
a second layer on the first layer, wherein the second layer at least partially fills the textured surface and the cracks so that the second layer is merged into the first layer with components of the first and second layers being hardly distinguishable from one another in a scanning micrograph.
22. The substrate of claim 21, wherein the second layer is selected from a group consisting of polysilsesquioxane, polyurethane, epoxy-functionalized silicone resin, and polyester-functionalized silicone resin.
23. The substrate of claim 21, wherein the first layer further comprises filler particles made of glass spheres and/or hollow glass spheres.
24. The substrate of claim 21, wherein the substrate is made of a zero-expansion material.
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DE201210109808 DE102012109808A1 (en) 2012-10-15 2012-10-15 Preparing composite material used in e.g. door of oven, comprises applying of sol gel layer prepared by mixing pigment particle and oxide particle on glass or glass ceramic substrate, and applying polymer layer on sol gel layer
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